@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ130_head
{
this:
np:hasAssertion
dgn-np:NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ130_assertion
;
np:hasProvenance
dgn-np:NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ130_assertion
a
np:Assertion
.
dgn-np:NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ130_provenance
a
np:Provenance
.
dgn-np:NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ130_assertion
{
miriam-gene:1139
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGN5b2375009857cf0475a3be8af2067a62
sio:SIO_000628
miriam-gene:1139
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ130_provenance
{
dgn-np:NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ130_assertion
dcterms:description
"[Recurrent microdeletions of chromosome 15q13.3 are causally associated with autism spectrum disorders (ASDs), suggesting that haploinsufficiency of CHRNA7, the gene that codes for the α7 nicotinic acetylcholine receptor (α7 nAChR) subunit, is an etiological mechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:22094647
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP939641.RAFTdoFv_R7gCHMa0_LJriFu64fYhOg2Ibg3HlNYgfuwQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:51+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}